Canonical Allele Identifier: CA1980214913
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585288G= , CM000673.2:g.67585288G= GRCh38
NC_000011.9:g.67352759G= , CM000673.1:g.67352759G= GRCh37
NC_000011.8:g.67109335G= NCBI36
NG_012075.1:g.6694G= , LRG_723:g.6694G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+47G= ENSP00000381604.1:n.336+47G=
ENST00000398606.10:c.336+47G= MANE Select ENSP00000381607.3:n.336+47G=
ENST00000646888.1:c.*52+47G= ENSP00000494477.1:n.*52+47G=
ENST00000398603.5:c.336+47G= ENSP00000381604.1:n.336+47G=
ENST00000398606.7:c.336+47G= ENSP00000381607.3:n.336+47G=
ENST00000467591.1:n.447+47G=
ENST00000494593.1:n.1131+47G=
ENST00000498765.5:c.399+47G=
NM_000852.3:c.336+47G= , LRG_723t1:c.336+47G= NP_000843.1:n.336+47G=
NM_000852.4:c.336+47G= MANE Select NP_000843.1:n.336+47G=